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Knee Replacement clinical trials

View clinical trials related to Knee Replacement.

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NCT ID: NCT02540902 Active, not recruiting - Knee Replacement Clinical Trials

Study of an All Polyethylene Tibial Component

Start date: October 2015
Phase: N/A
Study type: Interventional

This will be a prospective single cohort investigation of the Columbus all polyethylene tibia (Aesculap AG, Tuttlingen, Germany) used in total knee arthroplasty (TKA) surgery. The aim of the project is to determine post-operative outcome of the all polyethylene tibia up to two years.

NCT ID: NCT02527148 Completed - Knee Replacement Clinical Trials

A Trial of Mechanical Axis vs Kinematic Alignment in Total Knee Replacement

Start date: August 4, 2011
Phase: N/A
Study type: Interventional

This is a prospective, randomized, longitudinal study of the clinical outcomes of osteoarthritis patients treated by two different alignment philosophies for total knee replacement. In this study ShapeMatch® cutting guides will be compared to the conventional approach.

NCT ID: NCT02422251 Active, not recruiting - Knee Replacement Clinical Trials

Biomechanical Assessment of a High Congruency Knee Bearing

Start date: August 2015
Phase: N/A
Study type: Interventional

The aim of the project is to compare the biomechanics of three different bearing designs used in total knee replacement (TKR) implants. The bearing is the part in the middle of the knee implant that allows the metal tray attached to the shin bone (tibia) to move in relation to the metal part attached to the thigh bone (femur) and is usually made of plastic (high density polyethylene). There will be three different bearing types in the study, which all give different movements. This study will see which bearing is most like a natural knee and so which design gives the best function and feeling to patients with a TKR. 90 TKR patients from the Golden Jubilee National Hospital will be recruited and randomised to receive one of the three study bearings (30 in each group). In addition, a control group of 30 healthy individuals of similar age will be recruited for comparison. Before surgery and at 4 to 8 weeks and 1 year after their operation patients will attend biomechanical assessment sessions at the University of Strathclyde. The control group will attend the assessment session only once. In each of these sessions they will carry out a number of everyday tasks such as walking, moving from sitting to standing and going up and down stairs. These tasks will be measured using motion capture techniques. Reflective markers placed on each participant will be tracked by cameras so that their movements can be recorded. Force plates in the floor will record the forces during the tasks. Movement and force data will be analysed to see if any differences exist between the groups and show which bearing gives the most natural movement.

NCT ID: NCT02188199 Recruiting - Hip Replacement Clinical Trials

C3 Total Joint Patient Registry

Start date: May 2012
Phase: N/A
Study type: Observational [Patient Registry]

This study will assess the efficacy of products, implants, and procedures for knee and hip replacement.

NCT ID: NCT01743313 Terminated - Clinical trials for Hypercholesterolemia

Glucose Metabolism Disorders and Metabolic Syndrome Before and After Primary Hip and Knee Replacement

HyTe-2
Start date: April 2012
Phase:
Study type: Observational

Osteoarthritis patients undergoing primary hip and knee replacement are followed-up and changes in their glucose metabolism and other metabolic parameters (obesity, cholesterol levels) are examined. Persistent postoperative pain is examined as secondary outcome.

NCT ID: NCT01236729 Completed - Osteoarthritis Clinical Trials

Disability and Self-rated Health Following Primary Knee Replacement

Start date: December 2009
Phase:
Study type: Observational

Knee replacement is an effective treatment in late-stage osteoarthritis. It reduces pain and improves quality of life. There is, however, limited data concerning its results in older people and on its effect on how patients survive in regular activities of daily living (ADL), such as bathing and shopping. In this study, the results of knee replacement are evaluated from the point of view of disability in everyday activities and self-rated health. Moreover, association with ADL performance and clinical knee scores and severity of osteoarthritis are assessed.

NCT ID: NCT01021826 Completed - Hyperglycemia Clinical Trials

Perioperative Hyperglycaemia in Primary Total Hip and Knee Replacement

HyTe-1
Start date: December 2009
Phase: N/A
Study type: Observational

The purpose of this study is to analyze how common stress hyperglycaemia (abnormally high blood glucose) is in primary hip and knee replacement surgeries and which factors predispose to hyperglycaemia.

NCT ID: NCT00328939 Completed - Thromboembolism Clinical Trials

ARIXTRA Local Study For Registration In China.

Start date: May 2004
Phase: Phase 3
Study type: Interventional

This is a local registration study in China to compare the safety and efficacy of ARIXTRA to Enoxaparine in patients undergoing elective major hip or knee replacement or a revision of components.